Categories

Conditions Observed

Cancer

Acute Lymphoblastic Leukemia (ALL)
Childhood Acute Lymphoblastic Leukemia
Childhood Leukemia
Erythrocytosis
JAK2 V617F mutation
Myelodysplastic Syndrome
Myeloproliferative Disorder
Peripheral T cell lymphoma
Polycythemia Vera

Cardiovascular

Arginine-succinic aciduria
Atherosclerosis (hyperlipidemia)
Benefit of Niacin in Reducing Lipoprotein (a)
Cardiovascular Disease (Cholesterol Level)
Dysfunctional HDL
Familial Hyperlipoproteinemia Type III
Hereditary familial hypercholesterolemia
Hypercholesterolemia (Type B)
Jervell and Lange-Nielsen Syndrome
Narrowing of Blood Vessels (Stenosis)
Platelets (Highest Count)
Platelets (Lowest Count)
Prothrombin (G20210A Mutation)
Pulmonary Embolism
Venous Thromboembolism (VTE)

Cardiovascular and Cerebrovascular

Homocysteine Accumulation
Lipoprotein (a)

Clopidogrel

Response to Clopidogrel
 

Diabetes

Fasting Glucose Level Increase

Digestive system

Gilbert’s Syndrome

General

ALT / AST Index

Genetic diseases

A1 A2 Alloantigen Polymorphism
Alpha Antitrypsin Deficiency (AAT)
Alpha-2-Macroglobulin Polymorphism
Cholesterol Ester Transfer Protein Deficiency
Elliptocytosis
Factor II Deficiency (Prothrombin)
Factor VII Protease Polymorphism (Marburg)
Gamma-Glutamylcysteine Synthetase Deficiency
Glutathione Synthetase Deficiency
Hereditary angioedema
Hyperimmunoglobulin E (Hyper IgE) Syndrome
Leukocyte Adhesion Deficiency – Type 1
Mevalonate Kinase Deficiency
Multiple Sulphatase Deficiency (Austin’s Disease)
OKT4 deficiency
Upshaw Schulman Syndrome
Von Willebrand Disease
Wiskott-Aldrich Syndrome

 

Hematologic system

Activated partial thromboplastin time (aPTT)
Afibrinogenemia
Albumin
Alpha-Defensins Levels
Argininemia
Aspartate Aminotransferase (AST)
Atypical Hemolytic Uremic Syndrome (aHUS)
Benefit of Physical Exercise for HDL
Beta Thalassemia
Bilirubin
Bleeding Disorder (Platelets)
Blood Glucose Level
Carbamoyl Phosphate Synthetase I Deficiency
Circulating Glycated Hemoglobin (HbA1c)
Congenital Dyserythropoietic Anemia
Congenital Thrombotic Thrombocytopenic Purpura
Congenital afibrinogenemia
Crigler-Najjar Syndrome
D-dimers (Fibrin Degradation Products)
Deficiency of Vitamin K-Dependent Coagulation Factors
Essential Thrombocythemia
Excess Calcium in Blood
Factor V deficiency
Factor VII Deficiency
Factor XII Polymorphism
Factor XIII deficiency
Fanconi’s anemia
G6PD deficiency
Galactose Epimerase Deficiency
Glanzmann’s thrombasthenia
HDL (Cholesterol)
HDL Deficiency (Family)
Haptoglobin
Hemochromatosis
Hemolytic Anemia
Hemophilia – Factor VIII Deficiency
Hemophilia A
Hemophilia B
Hereditary Persistence of Fetal Hemoglobin (HPFH)
Hereditary Stomatocytosis
High Ferritin
High ferritin (in men)
Higher HDL on Low Carbohydrate Diets
Hyperbilirubinemia
Hyperhomocysteinemia
Hypoproteinemia
Idiopathic Hypereosinophilic Syndrome
Intermediate Beta Thalassemia
L-ferritin deficiency
LDL (Cholesterol)
Low Ferritin in Men
Low Ferritin in Women
Low ferritin in children under 2 years
Lower Hemoglobin Levels
Microcytic Anemia
Neuroferritinopathy
Ornithine Transcarbamylase Deficiency
Oxidized LDL
Paroxysmal Nocturnal Hemoglobinuria (PNH)
Platelet Count
Post-Transfusion Purpura (PPT)
Reduction in Factor VIII Activity (Coagulation)
Reduction in Factor XII Activity (Coagulation)
Shwachman-Diamond Syndrome
Sickle cell anemia
Spherocytosis
TIBC
Tendency to have Increased Eosinophils in Contact with Allergens
Thiamine-Responsive Megaloblastic Anemia
Thrombocytopenia
Thrombophilia (Factor V – Protein C)
Thrombophilia (Factor VII)
Transferrin
Triglycerides
Villejuif Hemoglobin
X Factor Deficiency

Hereditary diseases

Hereditary Sideroblastic Anemia

Hormones

Hepcidin

Immune system

Anti-Beta-2-Glycoprotein Antibody
Anti-DNA Antibody
Anticardiolipin Antib.
Antiphospholipid Antibody Syndrome
Antithrombin Deficiency
Autoimmune Lymphoproliferative Syndrome (ALPS)
Congenital Erythropoietic Porphyria (Gunther’s Disease)
Factor V Leiden Mutation
Familial hemophagocytic lymphohistiocytosis (HLH)
Human Leukocyte Antigen (HLA)
Lupus
Lupus anticoagulant
Malaria Resistance
Mannose Binding Protein Deficiency
Mutation of the SERPINE1 Gene (PAI-1)
Phenylketonuria
Primary Functional Neutrophil Disorder
Prolactin Promoter Polymorphism
Protein C Deficiency
Protein S Deficiency
Resistance to HIV (AIDS)
Resistance to Norovirus (NoV)
Type 2 X-linked Lymphoproliferative Syndrome
Wegener’s granulomatosis
X-linked Lymphoproliferative Syndrome (XLP)

Metabolic

Ceruloplasmin
Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency
Greater Insulin Sensitivity with Physical Exercise
Lactate dehydrogenase (LDH)
Methionine Adenosyltransferase Deficiency

 

Metabolic disorders

Cobalamin Intracellular Metabolism Disease
Dyslipidemia
Galactosemia
Homocystinuria
Hyperferritinemia
Low Ferritin
Myoadenylate Deaminase Deficiency

Methylation

MTHFR rs1801131
MTHFR 1298 mutation (rs1801131)
MTHFR 677 mutation (rs1801133)
MTHFR rs1801133

Need for Nutrients

Betaine
Iron

Personal characteristics

Toxic Sensitivity to Benzene
 

Pharmacogenetics

Warfarin

Respiratory system

Aspergillosis
Oxygen Volume (O2) Max (VO2 Max)

 

Skin

Basal Blade Disease
Erythropoietic Protoporphyria
Hyperchromias

Urinary system

Gout
Hematuria
Uric Acid (Concentration)

 

Vitamins

Vitamin B3 (Niacin)